Canonical Allele Identifier: CA2269131107

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683974C= , CM000679.2:g.61683974C=	GRCh38
NC_000017.10:g.59761335C= , CM000679.1:g.59761335C=	GRCh37
NC_000017.9:g.57116117C=	NCBI36
NG_007409.2:g.184586G= , LRG_300:g.184586G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682073.1:n.1812G=
ENST00000682453.1:c.3072G=	ENSP00000506943.1:p.Gly1024=
ENST00000682477.1:c.*2498G=	ENSP00000507075.1:n.*2498G=
ENST00000682589.1:n.8949G=
ENST00000682755.1:c.2850G=	ENSP00000507660.1:p.Gly950=
ENST00000682989.1:c.*163G=	ENSP00000507786.1:n.*163G=
ENST00000683039.1:c.3072G=	ENSP00000508303.1:p.Gly1024=
ENST00000683235.1:c.*487G=	ENSP00000507646.1:n.*487G=
ENST00000683535.1:n.1202G=
ENST00000684584.1:c.2235G=	ENSP00000508044.1:p.Gly745=
ENST00000684626.1:n.1318G=
ENST00000684769.1:c.1262G=	ENSP00000507691.1:n.1262G=
ENST00000259008.7:c.3072G= MANE Select	ENSP00000259008.2:p.Gly1024=
ENST00000259008.6:c.3072G=	ENSP00000259008.2:p.Gly1024=
NM_032043.2:c.3072G= , LRG_300t1:c.3072G=	NP_114432.2:p.Gly1024=
XM_011525332.1:c.3132G=	XP_011523634.1:p.Gly1044=
XM_011525333.1:c.3132G=	XP_011523635.1:p.Gly1044=
XM_011525334.1:c.3132G=	XP_011523636.1:p.Gly1044=
XM_011525335.1:c.3072G=	XP_011523637.1:p.Gly1024=
XM_011525336.1:c.3012G=	XP_011523638.1:p.Gly1004=
XM_011525337.1:c.2931G=	XP_011523639.1:p.Gly977=
XM_011525338.1:c.2649G=	XP_011523640.1:p.Gly883=
XM_011525332.3:c.3132G=	XP_011523634.1:p.Gly1044=
XM_011525333.3:c.3132G=	XP_011523635.1:p.Gly1044=
XM_011525334.2:c.3132G=	XP_011523636.1:p.Gly1044=
XM_011525335.3:c.3072G=	XP_011523637.1:p.Gly1024=
XM_011525336.2:c.3012G=	XP_011523638.1:p.Gly1004=
XM_011525337.2:c.2931G=	XP_011523639.1:p.Gly977=
XM_011525338.2:c.2649G=	XP_011523640.1:p.Gly883=
XM_017025200.1:c.2589G=	XP_016880689.1:p.Gly863=
XM_017025201.1:c.2589G=	XP_016880690.1:p.Gly863=
XM_017025202.1:c.1218G=	XP_016880691.1:p.Gly406=
XM_017025203.1:c.1218G=	XP_016880692.1:p.Gly406=
NM_032043.3:c.3072G= MANE Select	NP_114432.2:p.Gly1024=